Biostatistician - Clinical Trials

1 day ago


Boston, Massachusetts, United States Mass General Brigham Full time
Job Summary

This position involves statistical analysis and programming of large-scale international clinical trials. The successful candidate will have advanced formal training in statistics or biostatistics, including design and analysis of observational and experimental studies, and strong statistical computing skills.

Key Responsibilities
  • Collaborate with senior investigators to develop and perform statistical analyses for investigational protocols, subgroup and post-hoc projects, and registry databases.
  • Determine and/or verify correct statistical testing to be performed in each analysis request.
  • Possess a solid understanding of the purpose, objectives, and goals of each trial.
  • Rearrange data in a format that allows for accurate use and possible integration and pooling across trials.
  • Assure the maintenance of an up-to-date electronic archive recording data requests, statistical analyses, results, and data transmissions performed.
  • Maintain department service standards as outlined in the BWH Code of Conduct.
Requirements
  • Masters degree in biostatistics, statistics, or related field.
  • 3 years of related experience.
Preferred Qualifications
  • High proficiency in statistical computing; SAS experience strongly preferred.
  • Ability to work independently as well as part of a team.
  • Possess strong analytical skills.
  • Ability to prioritize assignments, multi-task, make decisions based upon sound principles, and independently problem solve.
  • Possess managerial skills in order to interact with both statistical staff and senior investigators.
  • Ability to draft plans to resolve inaccuracies or other problematic situations.
  • Excellent verbal and written communication skills.
  • Detail and process oriented.
  • Ability to manage multiple projects simultaneously, including both long-term and short-term projects.
  • Ability to make decisions related to issues in the statistical group pending final approval from the Director.
  • Ability to develop novel ways to coordinate, manage, and report data if required by new trials.
  • Demonstrated sound independent judgment and competencies in clinical research.


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